Use of AT(n) insertions in promoter elements for controlling the expression levels of coding sequences in plants
The present invention refers to the use of AT(n) insertions in promoter elements for controlling the expression levels of coding sequences in plants. The expression levels of the heat shock protein (Gmhsp17.6-L), when compared in resistant and susceptible individuals in the population, demonstrated that the largest expression levels per quantitative PCR were present in the individuals that contained the largest AT insertions in the promoter region. The invention also refers to gene expression cassettes containing promoter regions of the gene with different numbers of AT insertions fused to the GUS protein, for transforming soybean embryos.
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The present invention is related to the use of AT(n) insertions in specific points in the promoter region sequence towards controlling the expression levels of coding sequences in plants, which can be artificially up-regulated (upstream) or down-regulated (downstream), within certain limits.
BACKGROUND OF THE INVENTIONThe promoter region of a gene consists in a DNA sequence with generally 1 to 100 and 200 base pairs, upstream from the gene transcription start site and typically contains and/or is adjacent to one or more transcription factor binding sites. All the genes have transcription regulating upstream (above) and downstream (below) the transcription start site. The transcription factors recognize and bind to these regulating sequences, controlling the synthesis of the transcribed messenger RNA. These sequences include promoters, enhancers and regulating sequences. The promoters can be used in gene constructs, manipulated by means of genetic engineering, to overexpress, inhibit or modulate the expression of genes, in constitutive mode or induced by certain circumstances.
Various techniques for overexpressing genes are presently available in the field of Biotechnology, whereof the main technique comprises the construction of expression cassettes containing the constitutive promoter 35S, isolated from the cauliflower mosaic virus (CaMV—Cauliflower Mosaic Virus). There are however some exceptions to the use of this promoter in gene constructs. The use of a small sequence of viral DNA and the insertion thereof into the genome of a plant have proven experimentally the existence of a potential risk of genetic recombination between the genome of the virus that is infecting a plant and that of the transgenic plant, or more precisely, between the messenger RNA transcript. The risk would amount to the creation of a new virus strain, possibly of more virulent type.
The promoter 35S CaMV is considered promiscuous and functions effectively in all plants, as well as in green algae, yeasts E. coli. It has a modular structure with parts in common and interchangeable with promoters of other plant and animal viruses. It also has a recombination hotspot, flanked by multiple motives involved in the recombination process, similar to other recombination hotspots, including the borders of the T-DNA vector of Agrobacterium sp., frequently used in transgenic plants. This hotspot tends to split and bind to other DNAs and thereby increases the probabilities of horizontal gene transfer and recombination processes. Therefore, the potential risks are mutagenesis and carcinogenesis, due to insertions of the invasive exogenous DNA into the genomes, the reactivation of dormant viroses and the generation of new viroses, which will only be stable if they contribute some selective advantage over the wild type of the virus.
Partial or full transgenic events and/or inhibition of expression of endogenous homologues were observed using the promoter 35S CaMV (Napoli et al (1990) The Plant Cell 2: 279-289; Van der Krol at al (1990) Plant Cell 2 291-299). This inactivation occurs due to complex mechanisms involving methylations and epigenetic alterations (Renckens et al (1992) Mol. Gen. Genet. 233: 53-64; Neuhuber et al (1994) Mol. Gen. Genet. 244: 230-241; Meyer & Heidmann (1994) Mol. Gen. Genet. 243: 390-399; Thierry & Vaucheret (1996) Plant Mol. Biol. 32: 1075-1083. Although the actual mechanism that indicates certain sequences to the methyltransferases or other enzymes responsible for the epigenetic alterations remains unknown, there are hypotheses to suggest the involvement of interactions of dependent homologues between DNA-DNA, DNA-RNA and RNA-RNA (Grierson et al. (1991) Trends in Biotechnology 9: 122-123); Matzke & Matzke (1995) Plant Physiology 107: 679-685.
In the literature there is data evidencing that CaMV genes incorporated into canola chromosomes recombined with the genome of infecting viruses and produced new and more virulent viroses.
These recombinations between CaMV viroses involve promoter regions (Vaden & Melcher (1992) Virology 177: 717), and may take place between DNA and DNA or between RNA and RNA and often give rise to infections that are more severe than the parental counterparts (Mol. Plant-Microbe Interactions 5: 48, 1992).
The use of the promoter 35S CaMV further usually results in the expression of products of the exogenous gene at rates lower than 1% of the total protein. Some improvements in this promoter, such as the duplication of some sequences and the addition of enhancers increased the expression thereof, but for some applications the expression levels of the exogenous gene products need to be further increased.
In general, in experiments having been conducted using the constitutive promoter 35S CaMV to obtain genetically modified plants for the characteristic of tolerance to biotic and abiotic stresses, it is reported that although the tolerance is increased in some cases, one of the undesired effects derived from the use of this promoter is the reduction of size of the plants, whose growth and development are normally affected, resulting in small plants irrespective of the plant species that was transformed (Kasuga et al. (1999) Nature America Inc. 287-291).
Therefore, although some negative effects such as delay in plant growth may take place, strategies like the use of stress-induced promoters to control gene expression may prevent or mitigate such effects.
In another work, Gelvin et al. (Plant Molecular Biology Manual. Norwell, Mass.: Kluwer Acedemic Publishers, 1995) analyzed the expression of GUS directed by some promoters constructed with various combinations of regulating sequences of two genes of the bacterium Agrobacterium tumefaciens: opine synthase (ocs) and mannopine synthase (mas). And among the various combinations, a hybrid promoter formed by the triple repetition of the ocs gene activating sequence fused with mas activating elements and mas promoter region, named “(Aocs)3AmasPmas”, exhibited in transformed tobacco cells expression levels of the GUS marker gene that were 10 times larger when compared to cells containing the promoter CaMV 35S. This new promoter did not affect the transformation efficiency, however the high level of expression of the marker gene facilitated the identification of larger proportions of transformed cells. The expression levels were high in leaves, roots and various cell types. This promoter was also very active in manioc and pea plants, two crops difficult to transform using Agrobacterium sp. This group, further using this promoter “(Aocs)3AmasPmas”, described the success in studying the fast transcription of genes introduced (after 18 hours) into tobacco and corn plants, differently from the expression controlled by the promoter CaMV 35S, which activity is weak and does not allow any detection of genetic expression within this time span.
There is a further option of using stress-induced promoters for overexpression of genes in gene constructs, and in this regard the promoter rd29, isolated from Arabdopsis thaliana, is the most used in the search for plants with better tolerance to abiotic stresses. As a rule, these genetic constructs are always fused to genes of the family DREB (Dehydration Responsive Element Binding) that control the expression of genes in response to environmental stresses such as drought, salinity and low and high temperatures. In some works that used different plant species there were reported as the result of genetic transformation with induced stress promoters, plants that were more tolerant to abiotic stresses (Oono et al., (2003) The Plant Journal, 34: 868-887; Kasuga et al. (2004) Plant Cell Physiol 45(3):346-350.
Fuganti et al. (2004) used soybean genotypes resistant and susceptible to cyst nematode. The document contains the initial data on molecular markers that would be used in assisted selection of soybean genotypes resistant to the cyst nematode. However, there was not detected any type of molecular difference between the individuals having been tested, regarding the level of DNA sequence or expression of mRNA encoded by the gene.
Fuganti (Master's Thesis, State University of Londrina [Universidade Estadual de Londrina], 2004) presented the selection of resistant strains, using molecular markers associated with genes of resistance and of molecular characterization of genomic regions comprising those genes of interest. In this work there is not disclosed qualitative or quantitative data to indicate a possible correlation between the size of the AT(n) insertions in the gene promoter region and the resulting level of expression of its mRNA or protein. The present invention proposes the ability to control and/or to up-regulate or down-regulate the expression level of any provided that there are inserted into the promoter regions certain numbers of AT(n) insertions. Such proposal is neither presented nor tested in this work.
Fuganti (PhD Thesis, State University of Maringá [Universidade Estadual de Maringá], 2007) presented quantitative and qualitative data that indicates a possible correlation between the different sizes of the AT(n) insertion within the promoter region of the gene Gmhsp17.6-L and the level of expression thereof in response to various abiotic and biotic stresses (cold, heat, drought, salinity, infection by nematode juveniles). However, the possibility of up-regulating or down-regulating the expression level of any gene, which coding region may be fused to the promoter regions containing different AT(n) sizes, in the absence and/or presence of biotic and abiotic stresses was neither presented nor discussed.
Patent document No. US2005059623 provides methods of use of local heat, by means of controlled application of ultrasound, to control the expression of a therapeutic gene, fused to the heat shock protein (HSP) promoter, expressed in selected cells. The proposed invention is aimed at controlling and up-regulating or down-regulating the expression level of any gene fused to the promoter regions of a heat shock protein that has in its gene sequence different sizes of AT(n) insertions expressed in all the transformed cells. Biotic or abiotic stresses may be applied to the entire plant. There is not disclosed any indication of the role of the AT insertions in the control of the gene expression, or of the possibility of use thereof as a tool to regulate the expression of any gene, provided that the same are inserted into the promoter region thereof.
Patent document US2003190706 relates to an exogenous gene fused to a DNA sequence that exhibits promoter activity, which would promote an increase in the total amount of the gene product (proteins). This region with promoter activity was produced from mutagenic alterations including substitutions and deletions of nitrogenized bases. The present invention requires the use of a complete gene promoter, containing all the gene elements required to induce the synthesis of mRNAs. It is clear in the present invention that the control of the gene expression would result in levels differentiated according to the size of the AT(n) insertions, rather than random mutations in the promoter region of the gene.
Patent document EP1930423 discloses a promoter region of a heat shock protein, split into different final sizes, that is used in a system for the production of heterologous protein, whose expression levels are not controlled by means of other conventional promoters. In order to activate the expression there are used specific stresses, either abiotic or chemical. The present invention uses a previously existing variation in the genotypes studied, smaller than the 1000 bp fragment used in document EP1930423, and detected in the promoter region of the gene Gmhsp17.6-L. This variation is provided by the different numbers of AT(n) insertions in specific regions of the promoter, resulting in size variations between 312 bp (AT9) and 358 bp (AT33) depending on the AT(n) insertion.
U.S. Pat. No. 5,929,302 uses a temporal and tissue-specific promoter, which regulates the gene expression at the time of maturity, in tissues such as leaves and receptacles. The promoter was isolated from the dru gene itself, or from its homologue, in raspberries, to express chimeric genes. There is suggested the combination of this promoter with specific genes such as genes that regulate the change of color and flavor, genes of enzymes or catabolic products that modify plant cell processes, genes whose products affect the synthesis of ethylene, alternative fungal control genes and sucrose accumulating genes. The present invention proposes alterations in the promoter region of any gene, in order to alter the expression thereof in all cells and throughout the entire life cycle of the plant. The variation of the expression level of the gene product would be correlated with the different numbers of AT(n) insertions into the promoter, and consequently with promoters of different sizes. The invention proposes to control the expression of any gene containing these alterations.
Therefore, the present invention is innovative, as it differs from all presently existing methodologies available in the scientific literature to overexpress genes. To do so, the invention uses the insertion of an AT sequence with a greater and smaller number of repetitions, enabling the modulation of the levels of gene expression, increasing or reducing the same.
SUMMARY OF THE INVENTIONThe present invention refers to the use of AT(n) insertions in promoter elements for controlling the expression levels of coding sequences in plants. The invention also refers to gene expression cassettes containing promoter regions of the gene with different numbers of AT insertions fused to the GUS protein, to transform soybean embryos.
The present invention provides a method for regulating expression levels of coding sequences in plants comprising:
(i) stably transforming a plant cell with an expression cassette carrying AT(n) insertions within the promoter element operably linked to gene of interest.
(ii) culturing the stably transformed plant cell under plant cell growing conditions;
(iii) regenerating a transgenic plant having stably incorporated into its genome the cassette of (i);
Wherein said transgenic plant shows different levels of gene expression when compared to control plants.
The invention further provides expression cassettes comprising two promoter regions having different numbers of AT-insertions linked to the promoter region of Gmhsp17.6-L gene.
Another embodiment of the invention is process provided for obtaining genetically modified plants comprising AT(n)-insertions, wherein said method comprises:
(i) stably transforming a plant cell with an expression cassette carrying AT(n) insertions within the promoter element operably linked to gene of interest;
(ii) culturing the stably transformed plant cell under plant cell growing conditions;
(iii) regenerating a stably genetically modified plant.
The results suggest that the expression level of a certain gene can be artificially up-regulated (upstream) or down-regulated (downstream), within certain limits, by inserting, via genetic engineering tools, AT(n) repetition bases inside the promoter region.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings will be provided by the office upon request and payment of the necessary fee.
The present invention refers to the use of AT(n) insertions in promoter elements for controlling the expression level of coding sequences in plants. A comparison was made of the expression levels of the heat shock protein (Gmhsp17.6-L), among resistant and susceptible individuals in the population, and it was noted that the largest expression levels per quantitative PCR were present in the individuals containing the largest AT insertions in the promoter region. Gene expression cassettes were constructed containing promoter regions of the gene with different numbers of AT insertions fused to the GUS protein, to transform soybean embryos. The results of the experiments of the present invention suggest that the expression level of a certain gene could be artificially up-regulated (upstream) or down-regulated (downstream), within certain limits, by inserting, via genetic engineering tools, AT(n) repetition bases inside the promoter region. Hence, the technology developed in the present invention permits the control of the expression levels of genes, provided that the AT(n) repetition insertions are inserted in specific points in the sequence of the promoter region.
Based on prior studies seeking to identify molecular markers for use in assisted selection of soybean genotypes resistant to the nematode Meloidogyne javanaica, the microsatellite marker, SOYHSP 176, of the F bond group, presented high significance for the populations tested, explaining for the character number of cysts in the root, 43% of the phenotypic variation and for note in descriptive scale 70% of the variation. It is important to point out that the fragment amplified by this marker was only present in the susceptible individuals, being absent in the resistant individuals.
This marker was sequenced and after searching for similarities with other sequences of nucleic acids deposited in gene banks, this sequence revealed high homology with the promoter region of a low molecular weight heat shock protein (Gmhsp17.6-L), found in the soybean, and deposited at the GenBank (access number: M11317). Using the complete sequence of this gene available at the GenBank, new pairs of primers were designed, seeking to amplify the fragment in both genotypes.
The strategy was successful and fragments were obtained both in the susceptible individuals as in the resistant individuals. All the resulting fragments were cloned and sequenced, also showing homology with the same promoter region of the gene Gmhsp17.6-L. However, the alignment of the sequences showed that the resistant plants when compared to the susceptible plants, have in the promoter region of the gene, a greater insertion of microsatellite, characterized by AT(n) repetitions. Thus, the fragments originating from the resistant parental PI 595099, presented 15 and 13 AT additional repetitions when compared with the sequence of the gene Gmhsp17.6-L, available at the GenBank. On the other hand, the fragment originating from the susceptible parental BRS 133, has six AT repetitions less than the sequence available at the GenBank. These results were repeated for the resistant and susceptible individuals of the population resulting from this cross-breading which were also sequenced.
The alignment also indicated that all the fragments amplified had the sequence complementary to the primers of the microsatellite marker SOYHSP 176. Having established this, the question then arose: why did the amplification not occur in initially resistant plants, even though the annealing region of the microsatellite primers probably existed? One possibility would be the greater number of AT repetitions in the resistant individuals, provided the formation of some kind of tertiary structure, such as a hairpin, resulting in the difficulty of the primers to anneal during the process of amplifying the DNA polymerase and, consequently, inhibiting the formation of an amplicon in these plants.
It was believed that the insertion of a microsatellite inside the promoter region of this gene would deactivate it in the susceptible plants, since the marker SOYHSP 176 only amplified in these individuals. However, studies revealed that all the samples presented the insertion of a microsatellite, perhaps being the number of AT repetitions inside the promoter region that may be interfering in the soybean's response to the nematode. The presence of a greater or lesser insertion of repeated sequences inside the promoter region of the gene may deactivate, activate or even alter the expression levels of the protein controlled by this promoter.
According to literature, one of the main functions of these AT-elements repeated in the control of the gene expression of the heat shock proteins, is to facilitate the access of the RNA polymerase to the transcription start site, and also to exclude histones in order to facilitate the bond of the heat shock factors (HSFs), responsible for inducing the transcription. The heat shock proteins, according to literature, act in the cell as molecular chaperones, establishing nascent polypetide chains and assisting in their correct folding, re-establishing proteins and/or denatured membranes, and also performing an important role in the signal transduction.
Therefore, to test the hypothesis that the length of the insertion into the promoter region of the gene Gmhsp17.6-L is altering the expression levels of the protein Gmhsp17.6-L in resistant and susceptible individuals infected by M. javanica, the Ribonuclease Protection Assay was used. The results showed that all individuals, whether resistant or susceptible, and regardless of the treatment, inoculated or not with the nematode, express the protein. By virtue of the biological function of the AT sequences in gene regulation and the difference existing between the individuals regarding the number of repetitions inside the promoter, it was believed that the ribonuclease protection assay would reveal a difference of expression of the gene Gmhsp17.6-L in the different individuals, yet the results show that theoretically there is no difference in the expression of this gene in response to infection by the nematode, at least not at a level detectable by the technique used.
In the attempt to confirm these results, a new study was devised using a more precise and accurate technique to quantify the gene expression level, the PCR in real time (RT-PCR). Parentals, BRS 133 (susceptible) and PI595099 (resistant) and also three individuals of the susceptible population (256-S, 259-S and 266-S) and resistant (JF7002, JF7027 and JF7056) originating from this cross-breading, were inoculated with the nematode. Roots in the treatments inoculated and non-inoculated with Meloidogyne javanica, were collected for extraction of RNA total cDNA synthesis which was subsequently used in the RT-PCR reactions for relative quantification.
The results showed that all resistant and parental individuals, PI595099, and of the population, JF7002, JF7027 and JF7056, present a higher expression of the gene Gmhsp17.6-L in the inoculated treatment with the cyst nematode, Meloidogyne javanica. These individuals of the population are the same that, in sequencing, presented higher AT(n) insertion inside the promoter region of the gene. Our hypothesis is that, when being infected by the nematode, the plant produces some factor that interacts with the AT-rich region of the promoter of the gene Gmhsp17.6-L of the resistant plant, activating the transcription thereof which would have the function of a chaperone in the cell. In plants sensitive to the interaction of the factor such as the AT region, it would not occur in such an intense way, meaning that the expression levels of the protein Gmhsp17.6-L would be lower in the plants sensitive to the nematode.
Through the technology of the present invention it will be possible to regulate the expression levels of different genes, containing AT insertions of different sizes in specific points of the promoter region. It will also be possible to develop GM plants overexpressing or underexpressing the genes, in proportion to the size of the AT insertion, present in the promoter region.
EXAMPLES Biological MaterialThe constructs were developed using soybean genotypes, parental PI595099 and BRS133, resistant and susceptible, respectively, to the gall nematode, M. javanica. From this cross, in the F4 generation, the individuals 256-S, 259-S and 266-S, from the susceptible population and the individuals JF7002, JF7027 and JF7056 from the resistant population, were selected and used in the study.
The cultivar Pintado, susceptible to the nematode was also used in the transformation step, through particle bombardment, of soybean embryos using expression cassette constructed from different samples and containing different AT(n) insertions in the promoter region of the gene Gmhsp17.6-L (GenBank accession number: M11317).
Example 1: Isolation and Characterization of the Promoter and the Complete GeneUsing the complete sequence of the gene Gmhsp17.6-L, obtained from the initial sequencing of the amplified fragment of susceptible materials using microsatellite marker Soyhsp 176 primers, new primer sets were designed in order to obtain bands in all genotypes under analysis, given that, initially, only susceptible genotypes amplified the microsatellite marker SOYHSP 176 (
The primers (pSoyHsp_AleI F 5′CAC CGC GGT G GAA TTC TGA AAT TGG GTC TTT TTG3′ (SEQ ID NO: 4); pSoyHsp_NcoL_R 5′CCA TGG AAT GGG GAC ACT CGA GGT ATT3′ (SEQ ID NO: 5)) were synthesized in the beginning of the promoter region of the gene Gmhsp17.6-L, adding restriction sites for future cloning.
More new primer sets (pSoyHSP_PstI_F 5′GGG CTG CAG GAA TTC TGA AAT TGG GTC TTT TTG3′ (SEQ ID NO: 6); SoyHSPCL_R 5′CCC CCC GGG TTA ACC AGA GAT TTC TAT AGC CT3′ (SEQ ID NO: 7) were designed, in order to amplify the whole gene, from the beginning of the promoter to the stop codon in the coding region, and subsequently, verify the existence of other differences in the gene sequence, besides the AT(n) insertions of the promoter region between the genotypes susceptible and resistant to the gall nematode M. javanica.
The genomic DNA from seeds was extracted from all the analyzed samples. From each analyzed sample, approximately 50 mg of seeds, sliced in thin sections using a razor blade, were collected in a 1.5 mL microtube and 300 μL of extraction buffer was added. The material was grinded and an extra 700 μL of extraction buffer was added. The extraction buffer was prepared according to the protocol presented in the table below:
The solution was homogenized, using a vortex, for 30 s to 1 min and centrifuged for 4 min, at 16.000×g, at room temperature. The supernatant was transferred to a new 1.5 mL tube, submitted to a new centrifugation step at the same previous conditions and, once again, transferred to a new 1.5 mL tube.
In order to eliminate proteins, 0.1 mg of Proteinase K and 0.01 mM of CaCl2 was added to the samples and those were incubated in water bath at 37° C. for 90 min. 900 μL of cold isopropanol was added and, after incubation for 2 min, a centrifugation for 7 min 16.000×g was conducted. The supernatant was discarded and the pellet was dried for 90 min. The pellet was ressuspended in 300 μL of TE buffer (Tris-HCl 1M pH 8.0, EDTA 0.5 M pH 8.0) containing 40 μg/μL of RNase A and the samples were incubated once again in water bath at 37° C. for 90 min in order to eliminate the RNA. Following, a new precipitation step were conducted and, finally, the DNA pellet was ressuspended in 300 μL of TE buffer, quantified using spectrophotometry and its quality and integrity was verified in 0.8% agarose gel.
The PCR reactions in order to amplify the promoter region and the complete gene sequence, from all resistant and susceptible samples, were conducted using Perkin Elmer 9600 thermocycler and were constituted of: 30 ng of template DNA, 10× reaction buffer (100 mM of Tris-HCl pH 8.3, 500 mM of KCl and 400 μL of ultra pure water), 1.5 mM of MgCl2, 1.3 mM of dNTP, 1 U of Tag DNA polymerase and 5 μM of each of the F and R primers, using ultra pure water to complete up to the final volume of 10 μL.
The thermocycling program used to amplify the DNA samples was composed of an initial denaturation step at 94° C. for 7 min, followed by 30 cycles of denaturation at 94° C. for 1 min, annealing at 60° C. for 1 min and extension at 72° C. for 2 min. A 7 min at 72° C. cycle was conducted in the end. The products of amplification were separated in 1% agarose gel, prepared using 1×TBE buffer (108 g Tris base, 55 g boric acid, 40 mL EDTA 0.5 M pH 8.0 and distilled water to complete the final volume of 1 L) and stained in ethidium bromide (10 mg/mL). Images were obtained using the Kodak Digital DC 290 System.
The amplified fragments (
The obtained vector was used for Escherichia coli (DH10 B strain) cell transformation, through eletroporation. The eletrocompetent cells were prepared, obtaining isolated colonies through plate streaking from a glycerol stock. Following, a single colony was cultivated overnight in 10 mL of LB media—Luria Bertani (20 g of mixture of tryptone, yeast extract and NaOH for 1 L of distilled water) at 37° C., at 200 rpm (pre-inocule). 5 mL of pre-inocule were added to 500 mL of LB media, at 37° C. with rotation at 300 rpm, until an OD600 between 0.5 and 0.7 was reached. After this period, the cells were incubated on ice for 20 min and transferred to ice-pre-chilled 250 mL centrifuge tubes in aseptic manner. A centrifugation step at 4.278×g, for 15 min, at 4° C. was conducted, the supernatant was discarded and the pellet was ressuspended in 500 mL of cold 10% glycerol. A new centrifugation step under the same conditions was conducted, the supernatant was discarded and the pellet was ressuspended in 250 mL of cold 10% glycerol. One more centrifugation step was conducted and the pellet was ressuspended in 20 mL of cold 10% glycerol. The solution was transferred to 50 mL sterile tubes and centrifuged at 3997×g, for 15 min, at 4° C. As a final step, the pellet was ressuspended in 1 mL to 2 mL of 10% of cold glycerol. The eletrocompetent cells were aliquoted in 500 μL microtubes and stored in freezer at −80° C.
The eletroporation was conducted in MicroPulser (BioRad) eletroporator set to 2.5 kV, 25 μF, and pulse controller set at 200 or 400 ohms. 2 μL of the ligation reaction and 100 μL of the eletrocompetent cells were used. The rescue of the cells was obtained by cultivating the bacterial suspension in 1 mL of SOC media (0.5 g of yeast extract, 2 g of tryptone, 10 mM of NaCl, 2.5 mM of KCl, 10 mM of MgCl2, 10 mM of MgSO4, 20 mM Glucose and mL of distilled water), in 15 mL sterile Falcon tube, incubated at 37° C., for 1 h at 200 rpm. After this period, 300 μL of eletroporated cells were plated in solid LB media supplemented with ampicillin (100 μg/30 mL), containing IPTG/X-Gal (50 μl of IPTG—isopropyl-β-thiogalactopyranoside 0.1 M and 10 μL of X-Gal-1-bromo-4-chloro-3-indolyl-β-D-galactoside 50 mg/mL per plate). The plates were incubated at 37° C. overnight for colony growth. The selection of the recombinant clones was conducted using the lac Z system, which recombinant colonies presented white color and non-recombinant colonies, blue color due to the resulting product of the reaction between the lac Z gene product and the substrate (X-Gal).
Following, to confirm the cloning and the size of the fragments, a plasmidial DNA extraction was conducted by inoculation of single white colonies in 96-well microplates, containing 1 mL of CG media—Circle Grow (4 g of commercial mixture for 100 mL of water) and 100 μL/mL of ampicillin (50 μL de ampicillin at 100 mg/mL for 50 mL of CG media). The plate was sealed and the material incubated at 37° C., at 320 rpm, for 22 h.
Before proceeding to the plasmid extraction, a permanent culture of grown bacteria was obtained, containing 75 μL of CG media grown overnight and 75 μL of 50% sterile glycerol in sterile plates. This culture was stored in ultrafreezer at −80° C. to serve as stock.
Proceeding with the miniprep, in order to obtain sedimentation of the cells, the microplate was centrifuged for 6 min, at 1.310×g, at 10° C. The supernatant was discarded and the plate quickly inverted over absorbing paper. Following, 200 μL of GET (20% Glucose, 0.5 M EDTA pH 8.0, 1M Tris-HCl pH 7.4 and water to complete 500 mL) were added to each well, the plate was sealed and agitated using a vortex for 2 min to ressuspend the cells. A new centrifugation for 9 min, at 1.310×g, at 10° C. was conducted, the supernatant was discarded and the plate was inverted over absorbing paper and was dried.
65 μL of GET containing RNase A (10 mg/mL) were added to each well of the microplate. All the material was ressuspended using a vortex and transferred to a plate with “U” bottom. It was added then, to each well, 65 μL of NaOH 0.2N/SDS 1% (0.5 mL NaOH 4M+1 mL SDS 10%+ultra pure water to complete the volume of 10 mL). This solution was prepared just prior the beginning of the step in which it was going to be used. The plate was sealed; the material was mixed by inversion for 5 to 10 times and incubated for 10 min at room temperature. A quick centrifugation for a few seconds was conducted until there was no solution left in the adhesive seal.
To each well, it was added 60 μL of 3 M potassium acetate (KOAc) stored at 4° C., the plate was sealed, the material was mixed by inversion for 10 times and a 10 min incubation was conducted on ice. A centrifugation step of 15 min, at 1.310×g, at 4° C. was performed, and 80 μL of the supernatant was transferred to a Millipore® (MAGV N22) plate, previously fixed on top of a 250 μL “V” bottom polypropylene microplate. The plate was centrifuged for 5 min at 1.310×g, at 4° C., or until the whole volume was transferred to the bottom plate (V bottom). The Millipore® plate was removed and discarded and, to the filtered solution that was transferred to the “V” bottom plate, 80 μL of isopropanol were added.
The “V” bottom plate was sealed using alcohol-resistant adhesive and the material was mixed by inversion. A centrifugation step of 45 min, at 1.310×g, at 4° C., was conducted the supernatant was discarded by inverting the plate and 150 μL of cold 70% ethanol was added to each sample. The plate was centrifuged once again for 5 min, at 1.310×g, at 4° C. and, after the supernatant was discarded, the plate was inverted over absorbing paper and briefly spun down at 82×g, at 4° C. The plate was dried at room temperature covered by paper towel for 60 min and, finally, the DNA was ressuspended in 30 μL of ultra pure water. The plate was sealed and incubated at room temperature overnight for complete elution of plasmidial DNA. After this period, the plate containing the plasmidial DNA was stored in freezer at −20° C.
The samples, before being prepared for sequencing, were submitted to a digestion reaction using restriction enzymes, in order to confirm the presence of the insert and its size. The digestion reaction were composed 1.5 μL of React 3 enzyme buffer; 0.5 μL of EcoRI (10 U/μL); 5 μL of plasmidial DNA (˜10 ng) and 8 μL of ultra pure water, and incubated at 37° C., for 2 h. After this period, aliquots of the reaction were submitted to 1% agarose gel eletrophoresis.
The fragments were sequenced by a ABI Prism 3100 (Applied Biosystems) capillary sequencer, using ABI Prism BigDye terminator cycle sequencing (Applied Biosystems) kit on both orientation of the DNA double strand, using in different reactions and different sequencing experiments, M13 R and F primers. The sequencing reaction was preformed by placing 1.5 μL of DNA from each sample on the plate and 8.5 μL of the reaction mix which was prepared according to the protocol described in the table below.
The sequencing reactions were conducted using Applied Biosystem thermocycler, under the following conditions: 96° C. for 2 min, 30 cycles of 96° C. for 15 sec; 50° C. for 15 sec, and 60° C. for 4 min. Finally, the reaction for DNA precipitation was performed adding 80 μL of 75% isopropanol to each sample, followed by an incubation of 15 min at room temperature, protected from light, and a centrifugation step of 45 min, at 1.310×g.
The supernatant was discarded and the pellet was washed using 100 μL of 70% ethanol, followed of a centrifugation step of 15 min, at 1.310×g. The supernatant was discarded and, at room temperature and protected from light, the pellet was dried. For the sample application in the sequencing machine, the pellet was ressuspended in 10 μL of hi-formamide, and then, the samples were incubated on the thermocycler at 95° C. for 5 min, in order to cause DNA denaturation. The plate was immediately transferred to ice to avoid DNA reannealing and, after that, taken to the sequencing machine.
After the sequencing of the promoter region and the complete gene region, a sequence database search of biological sequences was conducted to verify the similarity between the obtained fragment and known DNA and protein sequences (FIG. 6). To accomplish this, the programs BLASTn and BLASTx (Altschul et al. (1997), Nucleic Acids Res. 25: 3389-3402) were used. Alignments of nucleotide sequences (
The parental genotypes PI595099 (resistant) and BRS133 (susceptible) were chosen for the RPA experiement. From the complete sequence of heat shock protein gene, Gmhsp17 0.6-L (GenBank accession number: M11317), present in soybean, a primer set was designed for the coding region (RPA2_F 5′GAC ATC ATC AAA CAA GAG AA3′ (SEQ ID NO: 8) and RPA2_R 5′TCT CTC CGC TAA TCT GAA3′ (SEQ ID NO: 2)).
The seed DNA extraction from the analyzed parental samples, the amplification of fragments through PCR, the cloning and the sequencing of the PCR-generated products were performed according to protocols previously described in details in the aforementioned items.
The total RNA from the parental PI595099 (resistant) and BRS133 (susceptible) were extracted from soybean roots submitted to two different treatments: inoculated and non-inoculated with M. javanica nematode eggs. The extraction was performed using the Trizol Reagent (Life Technologies) kit. The roots were grinded using a mortar and pestle in liquid nitrogen and transferred to autoclaved falcon tubes and store at the fume hood, containing 20 mL of Trizol. After homogenization, the samples were incubated for 5 min at room temperature (15-30° C.) 0.2 mL of chloroform for each 1 mL of Trizol was added and, after vigorous agitation for 15 sec, the solution was incubated at room temperature (15-30° C.) for extra 3 min. It was followed by a centrifugation step at 12.240×g, for 15 min at 4° C. The liquid phase, that contains the RNA, was transferred to a new falcon tube and precipitated using 0.5 mL of isopropanol for each 1 mL of Trizol initially used. The solution was incubated at room temperature (15-30° C.) for 10 min. A new centrifugation step at 12.240×g, for 10 min, at 4° C., was performed. The pellet formed on the bottom of the tube contains the precipitated RNA. The whole supernatant was removed and the RNA pellet was washed using 75% ethanol (1 mL de ethanol for each 1 mL of Trizol used). The solution was centrifuged at 4.285×g, for 5 min, at 4° C., and, once again, the whole supernatant (ethanol) was removed. 400 μL of DEPC water were added to the pellet in order to dissolve it (if necessary, the temperature can be elevated to 50-60° C. in order to dissolve the pellet). After the extraction, the total RNA was quantified by spectrophotometry; its integrity was verified in 2% agarose gel and, finally, stored in ultrafreezer at −80° C.
Initially, the plasmid containing the fragment of interest was linearized. The reaction containing 30.6 μL of DEPC water, 4 μL of buffer, 1 μg of the purified plasmid, 0.4 μL of BSA and 1 μL of the restriction enzyme ApaI, was incubated at 37° C., for 2 h using a thermocycler. After this period, the plasmid was purified using 1 volume of phenol, mixed using a vortex for 2 min and submitted to a centrifugation step at 11.750×g, for 10 min, at 4° C. Following, the aqueous phase was collected and ammonium acetate (NH4OAc) was added to a final concentration of 0.5 M. Three volumes of cold 95% ethanol were added and the solution was incubated at −20° C. for 1 h. A new centrifugation step at 11.750×g, at 4° C., for 15 min was performed and the supernatant was carefully discarded. The tube was opened; the pellet was dried for 5 min, and, following, ressuspended in 30 μL of DEPC water and stored in freezer at −20° C.
Obtaining Probes
The transcription reaction for obtaining probes was performed using the MAXIScript™ In Vitro Transcription (Ambion Inc.) kit. RNA polymerase T7 and P32-labelled phosphate dideoxinucleotide (CTP) were used. Initially, all kit reagents were thaw and kept on ice, with the exception of the Transcription Buffer®, which must be stored at room temperature. The transcription reaction with total final volume of 20 μL was performed in 1.5 mL microtube, at room temperature, according to the protocol described on the table below.
Following, all reagents were gently mixed in the microtube and the reaction was incubated at 37° C., for 1 h, using a thermocycler. 2 U of DNase I RNase-free was added and the reaction was incubated for 15 min, at 37° C. One volume of gel loading buffer (95% formamide, 0.025% bromophenol blue, 0.025% xylene cyanol, 0.5 mM EDTA, 0.025 SDS) was added to the reaction, the tubes were heated for 3-5 min at 85-95° C., and the whole sample was applied on 5% polyacrylamide gel, urea 8 M, 1×TBE buffer.
A final volume of 25 mL of gel was prepared, using 12.01 g de urea, following, 3.12 mL of 40% Acrylamide: bis-acrylamide (19:1) and 2.5 mL of 10×TBE. A small amount of water was also added avoiding exceeding the final volume of the gel. To dissolve the urea, the solution was kept in magnetic stirring system with heater and after was cooled down; transferred to a cylinder and the final volume of gel was completed with DEPC water. 12.5 μL of TEMED was then added and, at last, 156.2 μL 10% ammonium persulphate.
This solution was immediately applied to glass plates and a well comb was placed, allowing polymerization without moving the plates. A pre-treatment of these materials can be performed that consists in washing and treating with RNase AWAY® (Invitrogen—Life Technologies) the glass plates and the eletrophoresis chamber. On the smaller plate 1-3 mL Repel can be applied under the fume hood allowing the plates to dry for 5-10 min. This treatment facilitates the gel removal after the eletrophoresis.
Before proceeding to the eletrophoresis, the plates were cleaned, eliminating the excess of urea and after the removal of the well comb, the wells were washed, with the running buffer, with the aid of a syringe. A 20-30 min pre-run of the gel, using indicated voltage for the chamber, was performed, and following, the samples were applied. An eletrophoresis of approximately 2 h was conducted, at 200-300 volts, according to the size of the probe.
Only full-length probes were gel purified. To accomplish this, after eletrophoresis, the plates were opened, the gel was covered with plastic film, and an autoradiography film marked in order to guide the identification of the bands positions were exposed for approximately 1 h. Following, the film was developed in a dark room submerging it in developing solution for 5 min, removing the excess, submerging it in water for approximately 3 min for a wash and finally in fixing solution for 5 min. The film was then washed in water and air dried. The alignment of the film with the gel was performed in order to localize the position of the full-length transcripts. The areas of interest of the gel were removed and transferred to a microtube containing 350 mL of elution buffer (0.5 M ammonium acetate, 1 mM of EDTA, 2% SDS). The tubes containing the probes were incubated at 4° C., overnight, to maximize the probe recovery, which was stored at 20° C., until the time of hybridization. The kit for labeling the probes provided a positive control for monitoring its quality.
From the control DNA, the linearized pTRIPLEscript plasmid, containing the 250 bp insert of the rat β—actin gene, a probe was synthesized and hybridized to rat liver the total RNA, also provided in the kit. Two control tubes, containing only yeast total RNA, were used to verify the action of the RNase enzyme. This way, the enzyme positive control tube contained RNase and buffer, while the negative control tube contained only buffer without the enzyme.
Sample hybridization and digestion.
The Ribonuclease Protection Assay (RPA) was conducted using the HySpeed™ RPA—Hygh—Speed Hybridization Ribonuclease Protection Assay (Ambion Inc.) kit. To each microtube, the labeled probe was added (approximately, 100-800 pg of 250 nt or 1-10 fmol or 2−8×104 cpm with high specific activity) to the total RNA (20 mg). It was also added to the samples 30 mg of yeast total RNA to obtain a final 50 mg/sample. Two other enzyme control tubes were obtained containing 10 mL of yeast total RNA (50 mg) and one tube as probe positive control containing rat liver total RNA. In order to co-precipitate probe+sample, 0.5 M NH40 ac and 3 volumes of cold 95% ethanol was added and, after homogenization, the tubes were incubated for 15 min at −20° C. A centrifugation step at maximum speed (minimum of 8.160×g) for 5 min, at 4° C., was conducted. The supernatant was removed and the pellet was dried. 10 mL of HySpeed Hybridization Buffer® (pre-heated at 95° C.) were added to each sample and the tubes were immediately incubated at 95° C. (water bath or thermocycler). To dissolve the pellet, the samples were vortexed for a few seconds and returned to 95° C. When the pellet was completely dissolved, the tubes were incubated at 95° C. for 3 min and at 68° C. for 10 min. The temperature must be maintained at 68° C. and the transferring step must be under 30 sec. Initially, the HySpeed RNase digestion Buffer® was thawed, a mix of RNase A/T1 and buffer (dilution of 1:100-1 mL RNase in 99 mL of buffer) was prepared in appropriate volume of 100 mL for each sample and stored at room temperature. 100 mL of mix RNase A/T1+buffer were added to each sample and to the control tubes containing only yeast total RNA, 100 mL of HySpeed RNase Digestion® buffer without enzyme was added to one tube, and the complete mix with enzyme was added to the other control tube. The samples were vortexed and incubated at 37° C. for 30 min for digestion. 150 mL of HybSpeed inactivation/precipitation Buffer® was added to the samples which were briefly vortexed and the tubes were incubated in freezer at −20° C. for 15 min. Following the digestion, the samples were centrifuged for 15 min, at maximum speed, at 4° C., the supernatant was removed and the pellet ressuspended in gel loading buffer, usually, a volume of 9-10 mL. After pipette homogenization, the tubes were heated for 3-4 min at 90-95° C., and quickly transferred to ice to avoid renaturation. The samples were applied to 5% polyacrylamide gel, 8 M urea, diluted in 1×TBE buffer, and an eletrophoresis at 200-300 volts, for approximately 2 h, was performed for separation of the protected fragments. After the eletrophoresis, the standard procedures for film exposition and developing detailed in previously described protocols, were conducted (
For the expression study of the promoter of the gene Gmhsp17.6-L, using the RT-PCR technique, seeds from the materials PI595099, BRS133, 256-S, 259-S, 266-S, JF7002, JF7027 and JF7056 were plated on germination paper at growth chamber and, after eight days, the seedlings were transferred to plastic containers. At green house, these seedlings were infected with juvenile Meloidogyne javanica at infecting stage of development J2. The nematode population used was obtained from Centro Nacional de Pesquisa de Soja (Embrapa Soja) and was propagated on soybean plants from the cultivar Doko. The nematode egg extraction from root was obtained by grinding the material using a blender for 30 sec in a 0.5% hypochlorite solution. The roots were washed in water and the eggs were collected using a miniscreen with exclusion size 500. Following, the free eggs suspension were transferred to eclosion chambers set at 26° C., and, at every 24 h, the juveniles (J2) were collected and stored in a refrigerator. The juveniles J2 were quantified in a Peters Chamber. With the aid of a pipette, 664 J2/mL per plant were inoculated and at 1, 3 and 6 days pos infection, roots from three soybean plants of each of the eight materials under study were bulk collected and transferred to liquid nitrogen, for the inoculated ones and the non-inoculated with juveniles (control treatment). The roots were stored in ultrafreezer at −80° C., until the beginning of the RNA extraction experiment.
RT-qPCR Primer Design
The primers used for the real time PCR (SoyHspPSC_F 5′GCT GTG TGT CAT TGT CAT CGA A3′ (SEQ ID NO: 10); SoyHspPSC_R 5′CAC GGT CTA TTT CTT GCC TAC ATC3′ (SEQ ID NO: 11)) were designed with the aid of the Primer Express 2.0 (Applied Biosystems) program, using the sequence pos stop codon (TAA-nucleotide position 884) of the Gmhsp 17.6-L gene (GenBank accession number: M11317). These primers were used to amplify a fragment of approximately 80 bp. The chosen parameters applied to the Primer Express program to design the primers were: amplicon length between 50 bp and 150 bp (120 bp is recommended for RT-PCR), CG content between 40% and 60%, maximum of 4 G bases in tandem, primer Tm (Melting temperature) between 58° C. and 60° C., maximum difference between Tm of F and R primers of 1 degree Celsius, and up to 4 identical bases in tandem should be avoided. Following, in order to analyze the formation of primer dimers, the program OMIGA were used, observing the existence of a minimum of 6 free bp at the 3′ end.
Total RNA Obtaining for cDNA Synthesis
In order to perform real time PCR experiments, total RNA was extracted with Trizol reagent (Invitrogen—Life Technologies). Initially, 1 mL of Trizol per sample was aliquoted in Falcon tubes and heated at 55° C. The sample plant tissue was homogenized in liquid nitrogen and 0.1 g was aliquoted in tubes that were maintained in nitrogen. Following, 1 mL of heated Trizol were added to the samples, which were vortexed for 1 min, were quickly spun down and were incubated for 2 min at 55° C., followed by incubation on ice for 1.5 h. The samples were centrifuged at 4° C., for 20 min, at 16.000×g, the supernatant was transferred to tubes containing 200 μL of chloroform and the residues were discarded. The samples were shaken and incubated at room temperature (22-25° C.) for 2 min, followed by a centrifugation step at 16.000×g, for 30 min, at 4° C. The supernatant was transferred to a new tube and it was added ⅓ of the volume of 8 M LiCl. After shaking, the tubes were incubated in freezer at −80° C., for 1 h. In order to thaw the solution, the tubes were maintained for 1-3 min in water bath at 40° C., and centrifuged at 16.000×g, at 4° C., for 30 min. The supernatant was removed and discarded, avoiding disturbing the pellet which contains the RNA. It was added to each sample 400 μL of 75% ethanol and the tubes were gently inverted. A centrifugation step at 4° C. for 5 min, at 16.000×g was performed and the supernatant removed and completely discarded. It was added 100 μL of ultra pure water to the pellet and by gently flicking the tube, the pellet was dissolved (In case the pellet is not quickly being dissolved, an extra 100 μL of ultra pure water can be added, however, the volumes of sodium acetate and isopropanol at the next step should be doubled). Next, 10 μL of sodium acetate (3 M) and 100 μL of isopropanol were added and the tubes were gently inverted. The samples were incubated at −80° C., for 30 min, and transferred to water bath at 37° C. for 1-3 min, and centrifuged at 16.000×g, at 4° C., for 15 min. The supernatant was removed, 400 μL of 70% ethanol were added and the tubes were once again centrifuged 16.000×g, at 4° C., for 15 min. The supernatant was removed and discarded and, for 10 min, the pellet was dried at the bench. Finally, 50 μL of ultra pure water (or 100 μL, if the pellet is not quickly dissolved) was added and both the pellet and the solution were heated at 37° C., for 10 min, to facilitate the dissolution of the pellet. The RNA was quantified and stored in freezer at −80° C. For the reverse transcription reactions, the RNA was diluted and the cDNA synthesis was performed, using the reverse transcriptase enzyme (Moloney Murine Leukemia Virus—M-MLV). This way, 1.5 mg of total RNA was aliquoted in microtube, it was added DEPC water to a final volume of 9 mL, 6 mM of random primer was added to the reaction, followed by incubation at 80° C., for 3 min. After this period, the tubes were cooled down on ice and 14 mL of the mix was added to the samples. The mix was prepared according the protocol described on the table below.
The reactions were incubated using a thermocycler at 37° C., for 1 h, followed by a step of 10 min, at 65° C. The cDNA was stored at −20° C.
RT-qPCR
The PCR reactions were performed using the thermocycler 7300 Real Time System (Applied Biosystem), using the Platinum® SYBER® Green qPCR SuperMix UDG (Invitrogen—Life Technologies) kit, according to the manufacturer's instructions. As recommended by Applied Biosystems, an amplification efficiency curve was performed for the primer sets of the target gene Gmhsp 17.6-L and the endogenous control gene rRNA 18S (GenBank accession number: X02623.1), used for the samples normalization. The experiment plate was set with samples in triplicates for both genes. The curve provided a slope, used to calculate the amplification efficiency of the primers, which must be similar and close to 100% (value 1) for both genes. The amplification reactions for relative quantification were performed using a bulk of cDNA from the three days of harvest for each of the analyzed samples. It was performed, in separate experiments, two real time PCR experiments for the parental samples and two for the population samples. The parental lines BRS133 and PI595099 and the six resulting individuals from the susceptible populations, 256-S, 259-S and 266-S, and resistant, JF7002, JF7027 and JF7056, were analyzed for the nematode-inoculated treatment and non-inoculated treatment. The reaction were performed in triplicates and composed of 8.0 μL of ultra pure water, 0.5 μL of ROX, 12.5 μL of SYBER® Green qPCR SuperMix UDG and 2 μL of bulk cDNA (˜1.5 μg). The cycling parameters for the amplification reactions were: 50° C. for 2 min; 95° C. for 2 min; followed by 45 cycles of 95° C. for 15 sec, 60° C. for 30 sec and 72° C. for 30 sec, the data was collected at the extension step (72° C.). After the relative quantification was concluded, in order to verify the formation of primer dimers, inespecific amplifications and possible errors and contaminations, a dissociation curve was performed. The interpretation of the RT-PCR-generated data was performed using the SDS—Sequence Detection Systems (Applied Biosystems) software.
In these analyses, the calculation of the relative gene expression (RQ) was performed individually, comparing sample in separate, for nematode-inoculated and non-inoculated treatments, using as calibrator (value 1) the non-inoculated sample. The RQ value was calculated using the ΔCt method. This way, the level of gene expression (RQ) is calculated by subtracting the Ct of the target sample of each treatment with the endogenous control Ct, generating the Act. This value is subtracted from the ΔCt of the control sample (calibrator—value 1), resulting in the value of ΔΔCt. The RQ is obtained through the formula 2—ΔΔCt, in which 2 corresponds to the sum of the target gene efficiency (100%=1) and of the endogenous control (100%=1) obtained at the 100% efficiency curve (Livak and Schmittgen (2001), Methods 25: 402-408). The efficiencies of the target gene and endogenous gene must be close to 100%, but it is not necessary, they can be lower, however, they must be close. And, in this case, the value at formula 2—AACt, is substituted by the sum of the efficiencies of the target gene and the endogenous gene. For the analysis of the parental lines BRS133 and PI595099 in the treatments of inoculation and non-inoculation (
Once verified that the resistant individuals present a higher number of AT(n) insertions in the promoter region of the Gmhsp17.6-L gene and that these individuals, when submitted to RT-PCR, present high levels of this gene expression, when inoculated with the gall nematode M. javanica, it was decided to have expression cassettes constructed containing different number of AT insertions in the promoter region of the Gmhsp17.6-L gene. The objectives of utilization of these constructs were to observe if these promoters, with AT(n) insertions, could induce the expression of other genes and, also, evaluate the response of those genes, their activation or not upon different stresses. The cassettes were used to transform, using particle bombardment, soybean embryos from nematode-susceptible cultivars, BRS133 and Pintado. In the obtained construct, the promoter of the Gmhsp17.6-L gene is positioned prior the Gus gene which, after submission of the embryos to different stresses, had its expression detected through histochemical assay.
Expression cassettes containing the promoter region of eight analyzed samples, BRS133, P1595099, 256-S, 259-S and 266-S, JF7002, JF7027 and JF7056, were obtained, being 96 cassettes on total (12 of each of the materials). However, only two constructs were used in the next step of the study, the cassette pAG1/promotorGmhsp_BRS133, containing the amplified promoter region from the susceptible parental BRS133, with the fewer number of insertions, which is AT(9), and the cassette pAG1/promotorGmhsp_JF7027, containing the amplified promoter region from the individual from the resistant population JF7027, with AT(32). The plasmid pAG1 was chosen as template for construction of the expression cassettes. The designed strategy was removal of the act2 promoter from actin gene present in the plasmid and insertion of the amplified promoters from the materials to be analyzed, which are susceptible parental line BRS133 and the individual of the resistant population JF7027. This plasmid also presents the reporter gene Gus, which codes for the β-glucuronidase enzyme, which allows by visualization in the transgenic embryos, through histochemical assay, if the transformation process using those cassettes was successful. The plasmid pAG1 also contains the promoter (ahas 5), the coding sequence (ahas) and the terminator (ahas t) of the als/ahas gene, which codes for the enzyme acetolactate pyruvate lyase (AHAS)-acetolactate synthase (ALS) from Arabidopsis thaliana which due to a mutation in the position 653, confers resistance to herbicides Imidazolinones, class in which the herbicide Imazapyr (2-[4,5-dihydr-4-methyl-4-(1-methylethyl)-5-oxo-1H imidazol-2-yl]-3-pyridinecarboxylic) belongs to (Tu et al. (2004), Weed control methods handbook; London: Academic). This way, this gene enables, after transformation, the selection of positive plantlets in media containing the herbicide.
Obtaining Transgenic Plants Through Particle Bombardment
In order to obtain transgenic plants transformed with expression cassettes, pAG1/promotorGmHSP_BRS133 and pAG1/promotorGmHSP_JF7027, initially, a plasmidial DNA extraction was performed, according to previously described protocol. This procedure yielded a great quantity of plasmidial DNA sufficient to be used in the transformation process through biobalistic, gene gun method or particle bombardment. In this process, the introduction of the genetic material in plants is performed using microparticles, usually made from gold or tungsten, with diameter between 0.4-2.0 mm, coated with exogenous DNA. The particles were coated with the DNA molecules of interest, accelerated and shot at high speed due to a shock wave caused by a helium gas discharge under high pressure. When they hit the target cell or tissue, penetrating through the cell wall and the plasmatic membrane without disrupting them (Klein et al. (1987), Nature 327: 70-73), the exogenous DNA must dissociate from the microparticles by the action of the cellular liquid and be integrated to the plant genome. After being cultivated and regenerated in vitro, these transgenic tissues or cells will generate genetic modified plants (Brasileiro and Aragão (2001), Plant Biotechnol J. 3(3):113-121; Rech et al. (2008), Nat Protoc 3:410-418).
Seed Decontamination
Soybean seeds from the cultivars BRS133 and Pintado, both susceptible to the gall nematode, were used. After being weighted, the seeds were decontaminated in 70% ethanol for 10 min, followed by immersion in 1% sodium (V/V) for 20 min. In a laminar flow hood, the seeds were washed three times with autoclaved distilled water and embedded in water at double the volume of the seeds, being kept immersed for hydration for a period of approximately 16 h-18 h.
Embryo Isolation and Preparation of Support Plates for the Bombardment.
With the dehumidifier and the air conditioner on to lower room humidity, the embryos where isolated from the hydrated seeds. With the aid of sterile forceps and surgical blades, the seeds were incised and the embryonic axis removed and transferred to Petri dish containing distilled water to avoid drying. Following, with the aid of a stereomicroscope, the leaf primordia were excised, exposing the apical meristem region. The embryos were transferred to filter paper in a laminar flow hood to remove the water excess, which can lower the transformation efficiency behaving as a barrier to the particle, which will refract. For the bombardment, a centralized circle of 16 mm of diameter (death zone) was designed in small Petri dishes containing MS media (Murashige and Skoog Salt), 3% of sucrose and 0.8% of phytagel, pH 5.7, using a sterile forceps, sulcus were obtained outside the death zone. The embryos were positioned in the plates at the sulcus with the aid of a stereomicroscope, with the apical meristem region facing up. The carrier membrane support and the support cylinder were sterilized by fire and four rupture membrane set were separated and maintained immersed in isopropanol until utilization. The carrier membranes were assembled in their support.
Sterilization and Washing of the Tungsten Microparticles
In a microcentrifuge tube, 60 mg of M 10 tungsten microparticles were weighted, which is sufficient material for approximately 100 shots. To the microparticles, 10 mL of 70% ethanol were added; the solution was homogenized vigorously and kept on an agitator for 15 min in a speed sufficient enough to keep the movement. A centrifugation step at 15.000 g, for 5 min, was performed, and to avoid disturbing the settlement of the microparticle, with the aid of a micropipette, the supernatant was removed and discarded. 1 mL of sterile distilled water was added to the tube, the mixture was homogenized vigorously using an agitator and centrifuged once again at 15.000 g, for 5 min. The supernatant was discarded and the washing procedure was repeated twice. After the last wash and discard of the supernatant, the microparticles were ressuspended in 1 mL of 50% glycerol (V/V).
DNA Coating of the Tungsten Microparticles
In a 1.5 mL microcentrifuge tube, 50 μL of the microparticle suspension were aliquoted and submitted to a sonicator, for 15 min, for homogenization, avoiding, this way, the microparticles agglomeration and enabling a uniform precipitation. DNA equivalent to a minimum of 6 μg were added to the suspension, which was gently homogenized, with the aid of a micropipette. 50 μL of CaCl2 (2.5 M) was added to the solution and, after gentle homogenization, 20 μL of spermidin were added. After another homogenization, the solution was incubated for 10 min, at room temperature, under gentle rotation, in an adapted tube agitator. The tubes were spun down for 10 sec at maximum speed, the supernatant was removed and discarded, carefully, to avoid ressuspension of the microparticles. 150 μL of 100% ethanol was added; the solution was vigorously homogenized and centrifuged once again, for 10 sec, at maximum speed (spin). The supernatant was removed and the washing procedure was repeated once more. After the discard of the supernatant, in the last wash, 24 μL of 100% ethanol were added to the sample which was vigorously homogenized. Finally, aliquots of 3.2 μL of suspension were applied to the central region of each carrier membrane previously positioned on the membrane support. Each precipitation is sufficient to prepare 6 carrier membranes containing the microparticles coated with DNA. After microparticle application, the membranes were stored immediately on plate containing silica gel and were maintained in a dissecting chamber because the DNA-coated microparticles exposition to conditions of relative air humidity above 50% enables agglomeration, resulting in the reduction of the frequency of the exogenous gene expression.
Use of Gene Gun and Bombardment Experiment
The shots were targeted to the meristematic region of soybean seed embryos from cultivars BR133 and Pintado, both susceptible to the gall nematode, according to the protocol developed by Aragão et al. (Crop. Sci. 42: 1298-1302 (2002)), with few alterations. Prior the bombardment, the laminar flow hood was cleaned with 70% ethanol and sterilized with UV light for 15 min. The retention screens, the Petri dishes containing the embryos, the rupture membranes in set of four and immersed in isopropanol, and the carrier membranes containing exogenous DNA were maintained close to the operator. The valve of the helium gas cylinder was opened and the pressure was set at 1.200 psi. Following, the rupture membrane set (300 psi/membrane) was positioned in the far end of the high pressure helium gas chamber, the sealing screw was tightened, and the high pressure chamber was inverted to fit the vacuum chamber. The plates containing the material to be bombarded were positioned and, on the support cylinder, the retention screen and the carrier membrane support, containing the DNA-coated microparticles, were also positioned. Carefully, the support cylinder was positioned and the vacuum chamber was closed. The valve to allow the vacuum inside the chamber was slowly opened, until the pressure of 27 pol/Hg was reached, and at this time this valve was closed. The valve that allows helium gas inside the high pressure chamber was opened and, when the rupture membrane presented bending due to the presence of helium gas, the shot was performed, by pushing the trigger. After the shot, this valve was closed, while the valve that releases the helium gas from the high pressure chamber was opened. Following, the valve that releases the vacuum was slowly opened and the plate containing the embryos that were bombarded was removed from the equipment. At each bombardment, these procedures were repated. After each bombardment, most part of the embryos were transferred to different plates and submitted to abiotic and biotic stresses. Some embryos were, however, transferred to plates containing MS media supplemented with BAP 5 mg/mL (benzilaminopurine), 3% of sucrose 0.6% of agar and pH 5.7, in which were maintained for approximately 18 h protected from light, at 28° C., for regeneration induction.
Selection of Transgenic Embryos
The distinction between transgenic cells and non-transgenic cells can be performed through the introduction in the plant genome, separately or linked to the gene of interest in the same transformation vector, selection genes, which express a protein with enzymatic activity. According to the mode of action, the marker genes are classified as genes that confer resistant to antibiotics, genes that confer resistance to herbicides and marker genes with positive selection (Brasileiro and Dusi (1999), In: TORRES, A. C.; CALDAS, L. S.; BUSO, J. A. Ed. Cultura de tecidos and transformagão genética de Plantas. Brasília: Embrapa-SPI/Embrapa-CNPH, 1999. p. 679-735. v.2). The gene ahas belongs to the class of those which confers resistance to herbicides. This gene codes for a modified form of the acetohydroxil acid synthase (AHAS) enzyme, also known as acetolactate synthase (ALS). A mutation in the position 653 of the sequence resulted in a substitution of a serine by a asparagine, leading to a modified enzyme and that is not recognized by the herbicide class imidazolinones. Meristematic cells transformed with this gene are selected in the presence of the herbicide Imazapyr, in a process based on the systemic translocation of selective molecules to the meristematic regions and inactivation of the endogenous AHAS enzyme. Because the selective agent is localized in the apical meristem, the non-transgenic cells die and the survival of the transgenic cells which will develop into a plant is favored (Aragao and Brasileiro (2002), J. P. Physio, 14 (1)). This way, after the regeneration, some embryos were transferred to plastic cups containing the selective media MS, 3% of sucrose, 0.15 μM of Imazapyr herbicide, 0.8% of agar and B5 vitamin, pH 5.7, and grown for approximately 45 days on growth chamber, at 28° C., in a 16 h photoperiod, light intensity of 50 μmols m-2s-1 and relative humidity above 80%. The regenerated plantlets were, then, transferred to plastic cups containing sand:vermiculite (1:1) that were autoclaved and humidified with nutritive solution at pH 6.6. Later, the cups were covered with plastic bags, for acclimatization, and irrigated with nutritive solution according to necessity, grown on growth chamber for an extra 28-30 days. After this period of acclimatization, the plastic bags were removed so the plants could normally develop, until harvesting of samples for molecular analysis and identification of positive plants through PCR technique, using specific primers, was possible.
Experiments Using, Transgenic Embryos Submitted to Different Stresses
Embryos from the soybean cultivars BRS133 and Pintado, susceptible to the gall nematode and transformed with different expression cassettes, containing the promoter region of the Gmhsp17.6-L gene amplified from the parental susceptible line BRS133 (S—pAG1/promotorGmHSP_BRS133) and from the individual from the resistant population JF7027 (R—pAG1/promotorGmHSP_JF7027), were submitted to biotic stress, in this case, inoculation with juvenile J2 of M. javanica, and abiotic stress, such as heat, cold, salinity and dehydration (drought). Non-transgenic embryos (CN—negative control) and embryos transformed with only the pAG1 plasmid (CP—positive control) were submitted to the same treatments. The heat stress was applied, maintaining the embryos 25° C. (room temperature), 35° C. and 45° C. (in hothouse). Temperatures of 4° C. (refrigerator) and 15° C. (hothouse) were used in the cold stress. These stresses were applied with the embryos in solution, at time points of 2 h, 4 h and 24 h. The dehydration (drought) was performed in hothouse at 37° C., maintaining the embryos on filter paper, at time points of 2 h, 4 h and 6 h. For the salinity stress, the embryos were kept for 24 h at concentration of NaCl of 200 mM and 400 mM. The biotic stress was performed by maintaining the embryos in solution containing nematodes at J2 developmental stage (2.000 to 3.000 J2 per mL), for periods of 24 h, 48 h and 72 h.
Histochemical Assay in Embryos Transformed With Different Expression Cassettes and Submitted to Different Stresses
The expression product of the Gus gene can be used as a marker reporter of selection by detecting its enzymatic activity in plant tissues through histochemical assays. This qualitative method is based on the cleavage of the 5-bromo-4-chloro-3-indolyl-b-D-glucuronide (X-gluc) substrate, by the b-glucuronidase enzyme, generating, in the presence of oxygen, dimers that result in an insoluble blue precipitate. This methodology auxiliates gene expression regulation studies regarding tissue specificity, the isolation of promoters, the identification of transgenic plants and the optimization of transfer conditions (Brasileiro (1998), In: Brasileiro, A.C.M.; Carneiro, V.T.C. (ed.). Manual de transformagão genética de plantas. Brasília: Embrapa—SPI/Embrapa-Cenargen, 1998, p. 143-154; Aragao et al. (2000), Theor. Appl. Gen, 101:1-6). This way, embryos of both genotypes, BRS133 and Pintado, transformed with different cassettes, after being submitted to different stresses, were transferred to plates and the X-Gluc reaction buffer was added in enough volume to cover the samples. This buffer was prepared by diluting 8.5 mg of X-Gluc in 85 mL of dimetilformamide. Phosphate buffer (NaH2PO4—50 mM pH 7.0) was added to the volume of 17 mL and, at last, 17 mL of Triton X-100. The solution, after preparation, was stored in refrigerator. The plate containing embryos and buffer was sealed and incubated in the dark in hothouse at 37° C., for approximately 16 h. Following, the buffer was removed and 1 mL of 70% ethanol was added to stop the reaction. The samples were analyzed under a stereomicroscope, model SQZ-DS4-BI (Tecnival), and images were acquired to document the results. Histochemical assay results, after submission to stress, indicate that the cultivar BRS133 present stronger responses when the reagent X-Gluc is performed, since blue spots are visible in an obvious fashion and in restricted areas that represent cells that were transformed. This insoluble blue precipitate is the product of the Gus gene reaction present in the construct cassette, which coded for the β—glucuronidase, which reacts with the X-Gluc substrate, which in the presence of O2, forms dimmers that precipitate. When the embryo assay results from the cultivar Pintado were analyzed, in most of the stresses, positive blue spots were not detected. In this cultivar, the endogenous GUS expression was higher, resulting in a completely blue embryo, a result which interferes in the analysis. Background endogenous GUS activity in soybean embryos were reported in previous studies. Hu and collaborators (Plant Cell Reports, 9: 1-5, 1990) analyzed 52 different plant species, testing intrinsic GUS activity in leaves, fruit parts, seeds and embryos. In this study, soybean presented, in mature embryos from fresh fruits and mature embryos of dehydrated seeds, strong positive staining, result of the endogenous GUS activity. This way, the heat stress was applied by submitting transgenic embryos to temperatures of 25° C., 35° C. and 45° C., in hothouse, for periods of 2 h, 4 h and 24 h.
It can be concluded from the presented results for the cultivars BRS133 and Pintado, after the submission to the biotic and abiotic stresses, that the histochemical assay detected the presence of the marker gene Gus, however, high endogenous activity was also observed, especially, in the cultivar Pintado, suggesting that different materials presented distinct responses to the transformation process.
It is worth mentioning that the Gus expression is considered just as an evidence of transformation, being insufficient as definitive proof of integration of the Gus gene to the plant genome (Potrykus (1990), Physiologia Plantarum 79: 129-134). The definitive proof of integration of any exogenous DNA sequence is provided by genomic DNA hybridization using specific probes, through molecular biology techniques.
Claims
1. A method for regulating expression levels of coding sequences in plants comprising:
- (i) stably transforming a plant cell with an expression cassette comprising a modified promoter element operably linked to a coding sequence of interest,
- wherein said modified promoter element is a variant of an unmodified promoter element, said unmodified promoter element having the nucleotide sequence of SEQ ID NO: 21, and wherein said modified promoter element contains between 9 and 33 AT repetitions between the nucleotide positions that correspond to nucleotide positions 114 to 132 of SEQ ID NO: 21;
- (ii) culturing the stably transformed plant cell under plant cell growing conditions; and
- (iii) regenerating a transgenic plant having stably incorporated into its genome the cassette of (i).
2. The method according to claim 1, wherein said method is used for the control of nematodes in plants.
3. The method of claim 2, wherein the nematode is the gall nematode Meloidogyne javanica.
4. An expression cassette comprising a modified promoter element operably linked to a heterologous sequence,
- wherein said modified promoter element is a variant of an unmodified promoter element, said unmodified promoter element having the nucleotide sequence of SEQ ID NO: 21, and wherein said modified promoter element contains between 9 and 33 AT repetitions between the nucleotide positions that correspond to nucleotide positions 114 to 132 of SEQ ID NO: 21.
5. The expression cassette of claim 4, wherein said expression cassette is suitable for transforming soybean embryos.
6. The expression cassette of claim 4, wherein said expression cassette is used to control nematodes in plants.
7. The expression cassette of claim 6, wherein the nematode is the gall nematode Meloidogyne javanica.
8. A process for obtaining genetically modified plants comprising a modified promoter element, wherein said method comprises:
- (i) stably transforming a plant cell with an expression cassette comprising a modified promoter element operably linked to a coding sequence,
- wherein said modified promoter element is a variant of an unmodified promoter element, said unmodified promoter element having the nucleotide sequence of SEQ ID NO: 21, and wherein said modified promoter element contains between 9 and 33 AT repetitions between the nucleotide positions that correspond to nucleotide positions 114 to 132 of SEQ ID NO: 21;
- (ii) culturing the stably transformed plant cell under plant cell growing conditions; and
- (iii) regenerating a stably genetically modified plant.
9. The process according to claim 8, wherein the coding sequence operably linked to the modified promoter element is over-expressed.
10. The process according to claim 8, wherein the coding sequence operably linked to the modified promoter element is under-expressed.
11. The process according to claim 8, wherein said plants are resistant to a nematode.
12. The process of claim 11, wherein said nematode is the gall nematode Meloidogyne javanica.
13. The method according to claim 1, wherein the expression vector is derived from a pAG1 vector.
| 7126041 | October 24, 2006 | Helmer et al. |
| 20050155114 | July 14, 2005 | Hinchey |
| 1 452 596 | September 2004 | EP |
| 2005/019408 | March 2005 | WO |
- International Search Report for PCT/BR2008/000361 dated Jul. 16, 2009.
Type: Grant
Filed: Nov 28, 2008
Date of Patent: Jan 19, 2021
Patent Publication Number: 20140075594
Assignee: EMPRESA BRASILEIRA DE PESQUISA AGROPECUARIA - EMBRAPA (Brazilia)
Inventors: Renata Fuganti (Londrina), Alexandre Lima Nepomuceno (Londrina), Francismar Correa Marcelino (Londrina), Joao Flavio Veloso Silva (Londrina), Silvana Regina Rochenbach Marin (Londrina), Cesar Augusto Silveira (Londrina), Eliseu Binneck (Londrina)
Primary Examiner: Li Zheng
Application Number: 13/132,006
International Classification: C12N 15/82 (20060101); C07K 14/415 (20060101);
